These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

124 related articles for article (PubMed ID: 11857586)

  • 21. Idiopathic epilepsies with a monogenic mode of inheritance.
    Steinlein OK
    Epilepsia; 1999; 40 Suppl 3():9-11. PubMed ID: 10446744
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Possible association of a silent polymorphism in the neuronal nicotinic acetylcholine receptor subunit alpha4 with common idiopathic generalized epilepsies.
    Steinlein O; Sander T; Stoodt J; Kretz R; Janz D; Propping P
    Am J Med Genet; 1997 Jul; 74(4):445-9. PubMed ID: 9259383
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Genomic organization and chromosomal localization of the murine 2 P domain potassium channel gene Kcnk8: conservation of gene structure in 2 P domain potassium channels.
    Bockenhauer D; Nimmakayalu MA; Ward DC; Goldstein SA; Gallagher PG
    Gene; 2000 Dec; 261(2):365-72. PubMed ID: 11167025
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genetic variation of the human glycine receptor subunit genes GLRA3 and GLRB and susceptibility to idiopathic generalized epilepsies.
    Sobetzko D; Sander T; Becker CM
    Am J Med Genet; 2001 Aug; 105(6):534-8. PubMed ID: 11496371
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A splice-site mutation in GABRG2 associated with childhood absence epilepsy and febrile convulsions.
    Kananura C; Haug K; Sander T; Runge U; Gu W; Hallmann K; Rebstock J; Heils A; Steinlein OK
    Arch Neurol; 2002 Jul; 59(7):1137-41. PubMed ID: 12117362
    [TBL] [Abstract][Full Text] [Related]  

  • 26. C-terminal HERG mutations: the role of hypokalemia and a KCNQ1-associated mutation in cardiac event occurrence.
    Berthet M; Denjoy I; Donger C; Demay L; Hammoude H; Klug D; Schulze-Bahr E; Richard P; Funke H; Schwartz K; Coumel P; Hainque B; Guicheney P
    Circulation; 1999 Mar; 99(11):1464-70. PubMed ID: 10086971
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Mutation of a potassium channel-related gene in progressive myoclonic epilepsy.
    Van Bogaert P; Azizieh R; Désir J; Aeby A; De Meirleir L; Laes JF; Christiaens F; Abramowicz MJ
    Ann Neurol; 2007 Jun; 61(6):579-86. PubMed ID: 17455289
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genes and molecular mechanisms involved in the epileptogenesis of idiopathic absence epilepsies.
    Yalçın O
    Seizure; 2012 Mar; 21(2):79-86. PubMed ID: 22206818
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A human pancreatic islet inwardly rectifying potassium channel: cDNA cloning, determination of the genomic structure and genetic variations in Japanese NIDDM patients.
    Tanizawa Y; Matsubara A; Ueda K; Katagiri H; Kuwano A; Ferrer J; Permutt MA; Oka Y
    Diabetologia; 1996 Apr; 39(4):447-52. PubMed ID: 8777994
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Expression pattern in brain of TASK-1, TASK-3, and a tandem pore domain K(+) channel subunit, TASK-5, associated with the central auditory nervous system.
    Karschin C; Wischmeyer E; Preisig-Müller R; Rajan S; Derst C; Grzeschik KH; Daut J; Karschin A
    Mol Cell Neurosci; 2001 Dec; 18(6):632-48. PubMed ID: 11749039
    [TBL] [Abstract][Full Text] [Related]  

  • 31. CACNA1I is not associated with childhood absence epilepsy in the Chinese Han population.
    Wang J; Zhang Y; Liang J; Pan H; Wu H; Xu K; Liu X; Jiang Y; Shen Y; Wu X
    Pediatr Neurol; 2006 Sep; 35(3):187-90. PubMed ID: 16939858
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Ruthenium red inhibits TASK-3 potassium channel by interconnecting glutamate 70 of the two subunits.
    Czirják G; Enyedi P
    Mol Pharmacol; 2003 Mar; 63(3):646-52. PubMed ID: 12606773
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mutation screening of the chromosome 8q24.3-human activity-regulated cytoskeleton-associated gene (ARC) in idiopathic generalized epilepsy.
    Haug K; Kremerskothen J; Hallmann K; Sander T; Dullinger J; Rau B; Beyenburg S; Lentze MJ; Barnekow A; Elger CE; Propping P; Heils A
    Mol Cell Probes; 2000 Aug; 14(4):255-60. PubMed ID: 10970730
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Identification of native rat cerebellar granule cell currents due to background K channel KCNK5 (TASK-2).
    Cotten JF; Zou HL; Liu C; Au JD; Yost CS
    Brain Res Mol Brain Res; 2004 Sep; 128(2):112-20. PubMed ID: 15363886
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Idiopathic epilepsy of childhood and potassium ion channels.
    Dai AI; Wasay M
    J Pak Med Assoc; 2007 Aug; 57(8):415-8. PubMed ID: 17902527
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Allelic variants of human melatonin 1A receptor in patients with familial adolescent idiopathic scoliosis.
    Morcuende JA; Minhas R; Dolan L; Stevens J; Beck J; Wang K; Weinstein SL; Sheffield V
    Spine (Phila Pa 1976); 2003 Sep; 28(17):2025-8; discussion 2029. PubMed ID: 12973153
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Novel K+ channel genes in benign familial neonatal convulsions.
    Leppert M
    Epilepsia; 2000 Aug; 41(8):1066-7. PubMed ID: 10961643
    [No Abstract]   [Full Text] [Related]  

  • 38. Structural and mutational analysis of KCNQ2, the major gene locus for benign familial neonatal convulsions.
    Biervert C; Steinlein OK
    Hum Genet; 1999 Mar; 104(3):234-40. PubMed ID: 10323247
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Association of child absence epilepsy with T-STAR gene].
    Chen YC; Zhang YH; Lü JJ; Pan H; Jiang YW; Liu XY; Bao XH; Ding KY; Wu HS; Xu Km; Shen Y; Wu XR
    Zhonghua Yi Xue Za Zhi; 2003 Jul; 83(13):1134-7. PubMed ID: 12921630
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Functional expression of TASK-1/TASK-3 heteromers in cerebellar granule cells.
    Kang D; Han J; Talley EM; Bayliss DA; Kim D
    J Physiol; 2004 Jan; 554(Pt 1):64-77. PubMed ID: 14678492
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.